Three-dimensional structure of recombinant human interferon-gamma

Science. 1991 May 3;252(5006):698-702. doi: 10.1126/science.1902591.

Abstract

The x-ray crystal structure of recombinant human interferon-gamma has been determined with the use of multiple-isomorphous-replacement techniques. Interferon-gamma, which is dimeric in solution, crystallizes with two dimers related by a noncrystallographic twofold axis in the asymmetric unit. The protein is primarily alpha helical, with six helices in each subunit that comprise approximately 62 percent of the structure; there is no beta sheet. The dimeric structure of human interferon-gamma is stabilized by the intertwining of helices across the subunit interface with multiple intersubunit interactions.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Crystallization
  • Glycosylation
  • Humans
  • Interferon-gamma / chemistry*
  • Macromolecular Substances
  • Models, Molecular
  • Molecular Sequence Data
  • Protein Conformation
  • Recombinant Proteins
  • Sequence Homology, Nucleic Acid
  • X-Ray Diffraction

Substances

  • Macromolecular Substances
  • Recombinant Proteins
  • Interferon-gamma

Associated data

  • PDB/UNKNOWN